Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia

The hereditary cerebellar ataxias are a diverse group of neurodegenerative disorders primarily characterised by loss of balance and coordination due to dysfunction of the cerebellum and its associated pathways. Although many genetic mutations causing inherited cerebellar ataxia have been identified,...

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Detalles Bibliográficos
Autores principales: Becker, Esther B. E., Fogel, Brent L., Rajakulendran, Sanjeev, Dulneva, Anna, Hanna, Michael G., Perlman, Susan L., Geschwind, Daniel H., Davies, Kay E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114078/
https://www.ncbi.nlm.nih.gov/pubmed/21321808
http://dx.doi.org/10.1007/s12311-011-0253-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114078/
https://www.ncbi.nlm.nih.gov/pubmed/21321808
http://dx.doi.org/10.1007/s12311-011-0253-6

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